Busch Lab

ZMP

bag3

Ensembl ID:
ENSDARG00000039486
ZFIN ID:
ZDB-GENE-040801-40
Description:
BAG family molecular chaperone regulator 3 [Source:RefSeq peptide;Acc:NP_001003533]
Human Orthologue:
BAG3
Human Description:
BCL2-associated athanogene 3 [Source:HGNC Symbol;Acc:939]
Mouse Orthologue:
Bag3
Mouse Description:
BCL2-associated athanogene 3 Gene [Source:MGI Symbol;Acc:MGI:1352493]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa22301 Essential Splice Site Available for shipment Available now
sa38940 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa35490 Nonsense Mutation detected in F1 DNA Not yet available
sa6304 Nonsense Mutation detected in F1 DNA Not yet available
sa42208 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa22301
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000057689 Essential Splice Site 64 480 1 4
Genomic Location (Zv9):
Chromosome 13 (position 25710771)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 25356431
GRCz11 13 25486881
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAACAATCGCACAACGACGTGGAACGATCCGCGGCACGATACGAAAAAG[G/A]TAAGACCGACCCTGCTTTTGCTTTTGCGAAGTTGCGTTGTCAAACGCGAT
Long Flanking Sequence:
ATTGGAGGACAGATCTGACAGACTGTATGAAATGTGTTGATTCTGTCTGTATTTAGAAATGAACAGTAAAAAGAGCAACAAGTGCGCTCGGTCCAGTAAACCGTGGGGGAGGCGATTAAAGTCTCAGGAGCTCAGTGGATCTGTGTCTGGACGGTCAAGGGGTAATATTTGGTCACACGTGTGGGCGTAACAGTGATCCCTCAGCTAGAACTTTCTCGGTAGTCTTCGGACCTCGCTGCTTCGAGAAACCCGTCCCCATTGATAGTACGTCATCAAACGGACCCTTTAAAGCGTCTGTAGCGGCTGTAATGGCTCAATATTCGGGAGCGAAGCAATATCAGAGTATGAAAACACTGTCTCCGGTCGAAACGATGGCAACTAACGATCCTCTGCCACCTGGCTGGGAGATCAAAATTGACCCGCAGACAGGCTGGCCGTTTTTTGTGGATCACAACAATCGCACAACGACGTGGAACGATCCGCGGCACGATACGAAAAAG[G/A]TAAGACCGACCCTGCTTTTGCTTTTGCGAAGTTGCGTTGTCAAACGCGATCGGTTTTCCGGCGATTTCAAAATGCAGATCTGTGTGTGACTCTATTAACAGATTACTTCGGGTTGTGGCATTTTAGAGGCTGTTTCATCGATAAAAAGCAATTTTGCTGAGTGCGTAGGCTACGAGCCCACTCAGTACATCCAAAATCGTACTTGAGCAGACGCTGACTGTCTAGGGAAGATGAGCCACGCACTTGATATTCGCTTGAATCGCAGTCTCCTCTTGGAAACACAGCGCTTCGCGTGTATTTGAACGGCCTGGCGGAAGATGTTAGTGCACGGGCGAATATACGTTATATTAGTGTGATGATCTCAGGCGAAATGATTACTGTGTGACGCACTGCAGTCATATGTGAGAGTGTTAGAACGACTCCACAATGTTTATTTAAAGCCTCGAGAACTACGCACACTGCGCTTGTTCTCCACATCGCTGGAGCTACACAGCGCTAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38940
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000057689 Essential Splice Site 263 480 3 4
Genomic Location (Zv9):
Chromosome 13 (position 25719711)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 25365371
GRCz11 13 25495821
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAGAGCCCAGTCGCCAGTCATGGCTCAGATCATGGGAGAGAGGCCTCAG[G/A]TATGTGTGTTATTTATCAAGAGGATATTTTACTGAAAGATGAAAAAAAAA
Long Flanking Sequence:
AAATATTTTCTATTTTAATATATCTTAAAATGCAATTATTATTCCTGTGAAGGCAAAGCTGGATTTTCAACAGCTGTAGAAATTTGTAGTAAATTTATATGTTGTAAAAACTTTCTAATGTTTGTTTGTGACATTTATATAAATACAAGTGTTGTTAAGGTAAATTTTGACCAATTTAATGCAGACCCAAACTCTGTTTTTATTTACCAAAGGGATATCAACCACAAGGGACCCACCAACAAATCAGTGGCCTTCACCAGCAGCCCAGATCCAGCAATACAGGTCTCCGGGCAGGATACATCCCCATTCCGGTGATCCATGAGGGTGCCGGGGGGGTCTTGCCATCCCAGCTTAGCCAAAGTTCTCATCCCACTCGAGAAAAAATCTACCGTGAACAAGTGCCCATTCAGATTCAACAGAACCGTGCTGCCAGTCCCATCCAAGTCCCCTTAAGAGCCCAGTCGCCAGTCATGGCTCAGATCATGGGAGAGAGGCCTCAG[G/A]TATGTGTGTTATTTATCAAGAGGATATTTTACTGAAAGATGAAAAAAAAAAAACATAATCTAAAGAAAAGTGTAGCCATTGACATTGATAGAAGGAAAATTTTCATTTTAATGGCTACAGGTTTCTTCAAAATATCTCCTTTTGTGTTCAACAACAGAAAAAACCTTAAGCATGTTTGAACTAATGGAGGATGCATAAATAATGACATAATTTTCATTTTTGAATGAATTTTCTGTTCAAAAGTGCACTTAGCAATTTTTGAGAAATGCTTATGACACCAGTGTCTGACCGATACCCAAAACACACTTGCAGCCAATCTTCAGTAAGGGGTTTGTCTAGTAACACTAGTGGAGAATTCAAAAAGGGCATGCCATGACAATTTGTAACCTTTTGATTTAGTGGCTAATTTGTATGAATTTGTATGATCTCATTTGTTAGATTTATTATGGTTTGCTCATCCCCCAATGACGGTTGGGTTTAAGGGTGGGGTTGGATGCTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35490
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000057689 Nonsense 310 480 4 4
Genomic Location (Zv9):
Chromosome 13 (position 25721321)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 25366981
GRCz11 13 25497431
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATTCAAAGAGTGAGTGAAGTTCCCCAGCAGATACATCATCAGCCAGTA[C/T]AACAACAACAACAACCTACACAGCAGCCTCAGCCAAAAGCACAACCCTCC
Long Flanking Sequence:
CCTCTGGTGGATTTACATAAAAACAACAGGAGCGAATTGCACTCACGAGGGAAATTTGAAATCTCAAAAAGTGCACACAGTGGCCTCTAGTGAATTCGCGAAAACAAAAACTGCAAAACATACGTAGCTCCTGGGATGTATTTGGCGGTCTCCAGGAATGTATATCGAGGTACATTTTCAGAATTAGCCTGGGTTGTTATTTTTGGTACTTTCAAATAATATTGTTTGGCATAAATTGCTTCTTGCACCTCTAATGTTCATTTATGTCATATTTATTGTTATTATTAATCAAGTAATCATAAATAAGTAAATAAAAGAGGTACATATAAATGAAACTAAAGAGAATATGTTTTCATTTCTAGATGCAGCAACATATTGGACACACAGCCATACCTTCAAAAATTGAACATCCAGTTGAAGAAATCATCAGAGTACCTACATTTGAGGTTCCCATTCAAAGAGTGAGTGAAGTTCCCCAGCAGATACATCATCAGCCAGTA[C/T]AACAACAACAACAACCTACACAGCAGCCTCAGCCAAAAGCACAACCCTCCCCGCAGGTATCAGAAACATCCAATATTACCATACAAGTTCCTCCAGCACCAGAGCCCCAGGAAACAGCTGCTCCTCAAACGCCTCAAGAAGTCTCGTCCCCGCAACTCCAGCCTGAAGAGACTCTGGAACAAGATCTGAGCCACCCAGGACTGGTCAAAGTGCAGCAGATAGTGGAACGTGTGGAGAAGCTGGCACAGAATGTCAAGGGCTTCGATGGGAAGAAGAATGATAAAAGATACTTGGTACTGGAGGAGATGTTGACTAAAGAACTGCTAGCTCTGGACTCTGTAGATCCAGAAGGTCGTCCAGATGTGCGTCAGGCTCGGAGGGACGGCGTCCGCAGAGTTCAGAATATTCTAGACGAACTGGAGATGATCGGAGAGATGCAGGCTGGAAATGAGGCAAAAGGAGAGCAGAGTATGATTGACCAGTTGAACACAGAGAGAGTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6304
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000057689 Nonsense 314 480 4 4
Genomic Location (Zv9):
Chromosome 13 (position 25721333)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 25366993
GRCz11 13 25497443
KASP Assay ID:
554-5207.1 (used for ordering genotyping assays)
KASP Sequence:
TGAGTGAAGTTCCCCAGCAGATACATCATCAGCCAGTNNNNNNACAACAACAA[C/T]AACCTACACAGCAGCCTCAGCCAAAAGCACAACCYTCCCCGCAGGTATCA
Long Flanking Sequence:
TTACATAAAAACAACAGGAGCGAATTGCACTCACGAGGGAAATTTGAAATCTCAAAAAGTGCACACAGTGGCCTCTAGTGAATTCGCGAAAACAAAAACTGCAAAACATACGTAGCTCCTGGGATGTATTTGGCGGTCTCCAGGAATGTATATCGAGGTACATTTTCAGAATTAGCCTGGGTTGTTATTTTTGGTACTTTCAAATAATATTGTTTGGCATAAATTGCTTCTTGCACCTCTAATGTTCATTTATGTCATATTTATTGTTATTATTAATCAAGTAATCATAAATAAGTAAATAAAAGAGGTACATATAAATGAAACTAAAGAGAATATGTTTTCATTTCTAGATGCAGCAACATATTGGACACACAGCCATACCTTCAAAAATTGAACATCCAGTTGAAGAAATCATCAGAGTACCTACATTTGAGGTTCCCATTCAAAGAGTGAGTGAAGTTCCCCAGCAGATACATCATCAGCCAGTACAACAACAACAA[C/T]AACCTACACAGCAGCCTCAGCCAAAAGCACAACCCTCCCCGCAGGTATCAGAAACATCCAATATTACCATACAAGTTCCTCCAGCACCAGAGCCCCAGGAAACAGCTGCTCCTCAAACGCCTCAAGAAGTCTCGTCCCCGCAACTCCAGCCTGAAGAGACTCTGGAACAAGATCTGAGCCACCCAGGACTGGTCAAAGTGCAGCAGATAGTGGAACGTGTGGAGAAGCTGGCACAGAATGTCAAGGGCTTCGATGGGAAGAAGAATGATAAAAGATACTTGGTACTGGAGGAGATGTTGACTAAAGAACTGCTAGCTCTGGACTCTGTAGATCCAGAAGGTCGTCCAGATGTGCGTCAGGCTCGGAGGGACGGCGTCCGCAGAGTTCAGAATATTCTAGACGAACTGGAGATGATCGGAGAGATGCAGGCTGGAAATGAGGCAAAAGGAGAGCAGAGTATGATTGACCAGTTGAACACAGAGAGAGTCAAGGAGTTTTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42208
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000057689 Nonsense 338 480 4 4
Genomic Location (Zv9):
Chromosome 13 (position 25721405)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 25367065
GRCz11 13 25497515
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAAAGCACAACCCTCCCCGCAGGTATCAGAAACATCCAATATTACCATA[C/T]AAGTTCCTCCAGCACCAGAGCCCCAGGAAACAGCTGCTCCTCAAACGCCT
Long Flanking Sequence:
CTCTAGTGAATTCGCGAAAACAAAAACTGCAAAACATACGTAGCTCCTGGGATGTATTTGGCGGTCTCCAGGAATGTATATCGAGGTACATTTTCAGAATTAGCCTGGGTTGTTATTTTTGGTACTTTCAAATAATATTGTTTGGCATAAATTGCTTCTTGCACCTCTAATGTTCATTTATGTCATATTTATTGTTATTATTAATCAAGTAATCATAAATAAGTAAATAAAAGAGGTACATATAAATGAAACTAAAGAGAATATGTTTTCATTTCTAGATGCAGCAACATATTGGACACACAGCCATACCTTCAAAAATTGAACATCCAGTTGAAGAAATCATCAGAGTACCTACATTTGAGGTTCCCATTCAAAGAGTGAGTGAAGTTCCCCAGCAGATACATCATCAGCCAGTACAACAACAACAACAACCTACACAGCAGCCTCAGCCAAAAGCACAACCCTCCCCGCAGGTATCAGAAACATCCAATATTACCATA[C/T]AAGTTCCTCCAGCACCAGAGCCCCAGGAAACAGCTGCTCCTCAAACGCCTCAAGAAGTCTCGTCCCCGCAACTCCAGCCTGAAGAGACTCTGGAACAAGATCTGAGCCACCCAGGACTGGTCAAAGTGCAGCAGATAGTGGAACGTGTGGAGAAGCTGGCACAGAATGTCAAGGGCTTCGATGGGAAGAAGAATGATAAAAGATACTTGGTACTGGAGGAGATGTTGACTAAAGAACTGCTAGCTCTGGACTCTGTAGATCCAGAAGGTCGTCCAGATGTGCGTCAGGCTCGGAGGGACGGCGTCCGCAGAGTTCAGAATATTCTAGACGAACTGGAGATGATCGGAGAGATGCAGGCTGGAAATGAGGCAAAAGGAGAGCAGAGTATGATTGACCAGTTGAACACAGAGAGAGTCAAGGAGTTTTCATAACTGCTCAAAGAAGGCACACATTTGAGAACACTAATATAATCCCCATTCTTCTTTTTACTTGTGCAATTA
Associated Phenotype:
Not determined